A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832442



Internal ID22607377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210212128..210214323hg38UCSC Ensembl
chr2:211076852..211079047hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg382196
hg192196
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482052
Samples
Known GenesACADL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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